A novel TTN deletion in a family with skeletal myopathy, facial weakness, and dilated cardiomyopathy

BACKGROUND: Pathogenic variants in TTN (OMIM 188840), encoding the largest human protein, are known to cause dilated cardiomyopathy and several forms of skeletal myopathy. The clinical interpretation of TTN variants is challenging, however, due to the frequency of missense changes, variable testing...

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Detalles Bibliográficos
Autores principales: Roggenbuck, Jennifer, Rich, Kelly, Morales, Ana, Tan, Christopher A., Eck, Douglas, King, Wendy, Vatta, Matteo, Winder, Thomas, Elsheikh, Bakri, Hershberger, Ray E., Kissel, John T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Clinical Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6825852/
https://www.ncbi.nlm.nih.gov/pubmed/31489791
http://dx.doi.org/10.1002/mgg3.924

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6825852/
https://www.ncbi.nlm.nih.gov/pubmed/31489791
http://dx.doi.org/10.1002/mgg3.924

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